IgA nephropathy-specific expression of the IgA Fc receptors (CD89) on blood phagocytic cells

肾病 生物 受体 肾小球肾炎 免疫学 信使核糖核酸 分子生物学 单核细胞 外显子 抗体 免疫沉淀 粒细胞 Fc受体 基因 内分泌学 遗传学 糖尿病
作者
Shin‐ichi Toyabe,Yuh Kuwano,Kazuyoshi Takeda,Makoto Uchiyama,Toru Abo
出处
期刊:Clinical and Experimental Immunology [Oxford University Press]
卷期号:110 (2): 226-232 被引量:28
标识
DOI:10.1111/j.1365-2249.1997.tb08321.x
摘要

SUMMARY We analysed the biochemical features of receptors for the Fc-region of IgA (FcαR, CD89) on blood monocytes and granulocytes of patients with IgA nephropathy (IgAN). FcαR on monocytes of IgAN were found to have a higher Mr (60-80kD) than those of control monocytes (50–75 kD) and granulocytes (55–75 kD) in both IgAN and controls as shown by immunoprecipitation analysis. Removal of N-linked carbohydrates from FcαR on monocytes of IgAN revealed a 32–36 kD protein core, the Mr of which was still higher than that of controls (28–32 kD). When FcaL transcripts were analysed by reverse-transcription-PCR, only one prominent band was visualized in PCR products from IgAN monocytes. Since the results thus far show that IgAN monocytes express FcαR protein and mRNA differently from granulocytes and control monocytes, PCR products were then cloned and sequenced. The predominant band in PCR products from IgAN monocytes was identical to that of the FcαR a.l transcript, and an additional 10 transcripts containing five novel transcripts were obtained from granulocytes and control monocytes. In three transcripts, we found an insertion sequence between the S2 and EC1 domains, suggesting the existence of a new exon. These results suggest a predominant usage of FcαR a.l among various transcripts of FcαR in IgAN monocytes.
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